UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
A A A+ A- A0 A1 A2 A3 A4 A5 A6 A7 A8 A9 AA AB AC AD AE AF AG AH AI AJ AK AL AM AN AO AP AQ AR AS AT AU AV AW AX AY AZ
AM AMA AMB AMC AMD AME AMF AMG AMH AMI AML AMM AMN AMO AMP AMS AMT AMV AMY
selected terms: 578 page 1 of 6

1. (+)-4-Amino-3-isoxazolidinone
[An analogue of the amino acid D-alanine with broad-spectrum antibiotic and glycinergic activities. D-cycloserine interferes with bacterial cell wall synthesis by competitively inhibiting two enzymes, L-alanine racemase and D-alanine:D-alanine ligase, thereby impairing peptidoglycan formation necessary for bacterial cell wall synthesis. This agent may be bactericidal or bacteriostatic, depending on its concentration at the infection site and the susceptibility of the organism. In addition, D-cycloserine is an excitatory amino acid and partial agonist at the glycine binding site of the NMDA receptor in the central nervous system (CNS); binding to the central NMDA receptor may result in amelioration of neuropathic pain. ( NCI )] (UMLS (NCI) C0010590) =Amino Acid, Peptide, or Protein; Antibiotic =2-Amino-3-hydroxypropionic Acid;
[AM500] ANTITUBERCULARS =CYCLOSERINE 250 MG;
51. 32am
[Mandibular right third molar abutment mesial hemisection ( HL7V3.0 )] (UMLS (HL7) C1553675) =Medical Device =Artificial dentition;
2. (+)-6-[Amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl]-4-(3-chlorophenyl)-1-methyl-2(1H)-quinolinone
[An anticancer drug that inhibits the transformation of normal cells to cancer cells. It belongs to the family of drugs called enzyme inhibitors. ( NCI )] (UMLS (NCI) C1176289) Tipifarnib;
=Organic Chemical; Pharmacologic Substance
52. 4 aminosalicylic acid
[antitubercular agent often administered in association with isoniazid. ( CSP )] (UMLS (CSP) C0030125) =Organic Chemical; Pharmacologic Substance ;
=antitubercular agent;
salicylate
3. (+-)-2-Amino-N-(beta-hydroxy-2,5-dimethoxyphenethyl)acetamide Monohydrochloride
[The hydrochloride salt form of midodrine, a direct-acting prodrug and sympathomimetic agent with antihypotensive properties. Midodrine is converted to its active metabolite, desglymidodrine by deglycination reaction. Desglymidodrine selectively binds to and activates alpha-1-adrenergic receptors of the arteriolar and venous vasculature. This causes smooth muscle contraction and leads to an elevation of blood pressure. Desglymidodrine diffuses poorly across the blood-brain barrier, and is therefore not associated with effects on the central nervous system. ( NCI )] (UMLS (NCI) C0733394) 1-(2',5'-Dimethoxyphenyl)-2-glycinamidoethanol Hydrochloride;
MIDODRINE HYDROCHLORIDE;
MIDODRINE HYDROCHLORIDE PREPARATION;
Midodrine Monohydrochloride =Organic Chemical; Pharmacologic Substance =MIDODRINE;
=MIDODRINE HYDROCHLORIDE 2.5 MG;
MIDODRINE HYDROCHLORIDE 5 MG;
MIDODRINE HYDROCHLORIDE 10 MG
53. 4'-Amino-6-hydroxyflavone
[A compound that inhibits the Protein-Tyrosine Kinase Activity of p56lck. ( NCI )] (UMLS (NCI) C0644340) =Organic Chemical; Pharmacologic Substance
4. (--)-2Amino-3-)3,4-dihydroxyphenyl)propanoic Acid
[naturally occuring form of DOPA and precursor of dopamine; used as an antiparkinsonian agent; unlike dopamine it can be administered orally. ( CSP )] (UMLS (NCI) C0023570) =Amino Acid, Peptide, or Protein; Pharmacologic Substance; Neuroreactive Substance or Biogenic Amine ;
=[CN500] ANTIPARKINSON AGENTS;
dihydroxyphenylalanine =LEVODOPA 100 MG;
LEVODOPA 200 MG;
LEVODOPA 250 MG;
Carbidopa 12.5 MG / entacapone 200 MG / Levodopa 50 MG Oral Tablet;
LEVODOPA 150 MG
54. 4-(Aminomethyl)benzenesulfonamide Monoacetate
[The acetate salt form of mafenide, a synthetic sulfonamide analog of para-aminobenzoic acid (PABA) with topical anti-infective activity. Mafenide acetate competes with PABA for the bacterial enzyme dihydropteroate synthase, thereby preventing the incorporation of PABA into dihydrofolic acid, thereby interferes with normal folic acid metabolism. As a result de novo synthesis of pyrimidines, which requires folate metabolites, is impeded and subsequently DNA synthesis is affected. Mafenide acetate is bacteriostatic against many gram-negative and gram-positive organisms, including Pseudomonas aeruginosa and certain strains of anaerobes. ( NCI )] (UMLS (NCI) C0024453) =Organic Chemical; Pharmacologic Substance =MAFENIDE;
[DE101] ANTIBACTERIAL, TOPICAL =MAFENIDE ACETATE 8.5 %;
MAFENIDE ACETATE 50 GM;
5. (4-Amino-1-hydroxybutylidene)bisphosphonic Acid
[bone resorption inhibitor. ( CSP )] (UMLS (NCI) C0102118) =Organophosphorus Compound; Pharmacologic Substance ;
=inhibitor/antagonist;
biphosphonate;
[HS900] HORMONES/SYNTHETICS/MODIFIERS, OTHER;
=ALENDRONATE 70 MG;
ALENDRONATE 35 MG;
ALENDRONATE 10 MG;
ALENDRONATE 5 MG;
ALENDRONATE 40 MG;
55. 4-Amino-1-beta-D-ribofuranosyl-1,3,5-triazin-2(1H)-one
[pyrimidine analog that inhibits DNA methyltransferase, impairing DNA methylation, also an antimetabolite of cytidine, incorporated primarily into RNA; has been used as an antineoplastic agent. ( CSP )] (UMLS (NCI) C0004475) =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance
6. 1 aminocyclopentyl 1,3 dicarboxylate
[ ] (UMLS (CSP) C0044270) =Organic Chemical; Pharmacologic Substance ;
56. 4-Amino-10-methylfolic Acid
[folic acid antagonist that acts by inhibiting the synthesis of nucleic acids, thymidylate, and protein; used as an antineoplastic in a wide variety of malignancies, and as an antipsoriatic and antirheumatic. ( CSP )] (UMLS (NCI) C0025677) =Organic Chemical; Pharmacologic Substance ;
=4-Aminofolic acid;
[AN300] ANTINEOPLASTICS, ANTIMETABOLITES;
[AN000] ANTINEOPLASTICS;
antifolate;
pteridine;
=METHOTREXATE SODIUM
7. 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(2-furanylcarbonyl)piperazine
[1-(4-amino-6,7-dimethoxy- 2-quinazolinyl) -4-(2-furoyl) piperazine. ( CSP )] (UMLS (NCI) C0032912) =Organic Chemical; Pharmacologic Substance ;
=antihypertensive agent;
PIPERAZINE;
quinazoline;
[CV150] ALPHA-BLOCKERS/RELATED =Terazosin;
DOXAZOSIN;
PRAZOSIN HYDROCHLORIDE;
PRAZOSIN 5 MG;
PRAZOSIN 1 MG
57. 4-Amino-2(1H)-pyrimidinone
[2-keto-4-aminopyrimidine, one of the 5 major bases (with adenine, guanine, uracil, and thymine) which are a component of nucleic acids. ( CSP )] (UMLS (NCI) C0010843) =Organic Chemical; Biologically Active Substance =Pyrimidinones;
aminopyrimidine;
nucleobase;
=4-Amino-5-fluoro-2(1H)-pyrimidinone;
1(3-hydroxy-2-phosphonomethoxypropyl) Cytosine
8. 1-(aminomethyl)cyclohexaneacetic Acid
[A substance that is being studied as a treatment for relieving hot flashes in women with breast cancer. It belongs to the family of drugs called anticonvulsants. ( NCI )] (UMLS (NCI) C0060926) =Organic Chemical; Pharmacologic Substance ;
=Acetic Acids;
[CN400] ANTICONVULSANTS =GABAPENTIN 100 MG;
GABAPENTIN 300 MG;
GABAPENTIN 400 MG;
GABAPENTIN 600 MG;
GABAPENTIN 800 MG;
GABAPENTIN 250 MG/5ML
58. 4-Amino-2-(ethoxymethyl)-alpha,alpha-dimethyl-1H-imidazo[4,5-c]quinoline-1-ethanol
[An imidazoquinolinamine and Toll-like receptor (TLR) agonist with potential immune response modifying activity. Resiquimod exerts its effect through TLR signaling pathway by binding to and activating TLR7 and 8 mainly on dendritic cells, macrophages and B-lymphocytes. This induces the nuclear translocation of the transcription activator NF-kB as well as activates other transcription factors. This may lead to an increase in mRNA levels and subsequent production of cytokines, especially interferon-alpha (INF-a) and other cytokines, thereby enhancing T-helper 1 (Th1) immune responses. In addition, topical application of resiquimod appears to activate Langerhans' cells leading to an enhanced activation of T-lymphocytes. Due to its immunostimulatory activity, this agent may potentially be useful as a vaccine adjuvant. ( NCI )] (UMLS (NCI) C0965594) Resiquimod =Organic Chemical; Pharmacologic Substance ;
9. 1-Amino-2,4-dibromo-9,10-anthracenedione
[A synthetic, light sensitive, red powder that is insoluble in water and soluble in many organic solvents. It is used as both an intermediate for the production of anthraquinone dyes and as a starting material for the manufacture of vat dyes. The primary route of potential human exposure to 1-amino-2,4-dibromoanthraquinone is dermal contact. It is reasonably anticipated to be a human carcinogen. (NCI05) ( NCI )] (UMLS (NCI) C0626387) =Organic Chemical
59. 4-Amino-3-(4-chlorophenyl)-butanoic Acid
[A synthetic chlorophenyl-butanoic acid derivative used to treat spasms due to spinal cord damage and multiple sclerosis, muscle-relaxing Baclofen acts as a gamma-aminobutyric acid (GABA) agonist specific for GABA-B receptors. It acts at spinal and supraspinal sites, reducing excitatory transmission. (NCI04) ( NCI )] (UMLS (NCI) C0004609) =Amino Acid, Peptide, or Protein; Pharmacologic Substance
10. 1-Amino-2-methyl-9,10-anthracenedione
[A synthetic, red powder that is insoluble in water and soluble in acetone, ethanol, ether, benzene, chloroform and acetic acid. It is used almost exclusively as a dye and dye intermediate for the production of a variety of anthraquinone dyes. The primary routes of potential human exposure to 1-amino-2-methylanthraquinone are inhalation and dermal contact. However, human exposure is limited because this compound is no longer produced in the United States. It is reasonably anticipated to be a human carcinogen. (NCI05) ( NCI )] (UMLS (NCI) C0044271) =Organic Chemical
60. 4-Amino-3-[[4'-((2,4-Diaminophenyl)azo)(1,1'-Biphenyl)-4-yl]azo]-5-Hydroxy-6-(Phenylazo)- 2,7-Naphthalenedisulfonic Acid, Disodium Salt
[A Benzidine-based azo dye that is metabolized to free Benzidine in vivo. Direct black 38 is primarily used for the dyeing of textiles, leather and paper. Benzidine and its metabolic derivatives have been detected in the urine of workers exposed to Benzidine-based dyes. Exposure to this dye is strongly associated with the occurrence of bladder cancer. (NCI05) ( NCI )] (UMLS (NCI) C0058437) =Organic Chemical; Indicator, Reagent, or Diagnostic Aid ;
11. 1-amino-3,5-dimethyladamantane Hydrochloride
[The hydrochloride salt form of memantine, a moderate affinity, noncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist. Memantine hydrochloride exerts its effect by binding to the cation channels on the NMDA receptor located in the central nervous system, thereby blocking the NMDA receptor and preventing the binding of the excitatory amino acid glutamate. This results in a reduction of abnormal excitement in the brain, which is often seen in Alzheimer's disease. Memantine hydrochloride also acts as an antagonist at the 5HT 3 receptor and the nicotinic receptor. ( NCI )] (UMLS (NCI) C0771988) Ebixia;
MEMANTINE HYDROCHLORIDE =Organic Chemical; Pharmacologic Substance ;
61. 4-Amino-5-fluoro-2(1H)-pyrimidinone
[fluorinated cytosine analog that is used as an antifungal agent. ( CSP )] (UMLS (NCI) C0016278) =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance ;
=[AM700] ANTIFUNGALS;
4-Amino-2(1H)-pyrimidinone;
pyrimidine analog;
halocarbon compound =FLUCYTOSINE 250 MG;
FLUCYTOSINE 500 MG;
12. 1-Amino-6,17-dihydroxy-7,10,18,21-tetraoxo-27-(n-acetylhydroxylamino)-6,11,17,22-tetraazaheptaeicosane
[natural product isolated from Streptomyces pilosus; it forms iron complexes and is used as a chelating agent, particularly in the mesylate form. ( CSP )] (UMLS (NCI) C0011145) =Organic Chemical; Biologically Active Substance; Indicator, Reagent, or Diagnostic Aid =chelating agent;
Hydroxamic Acids;
hydroxamate;
[AD300] HEAVY METAL ANTAGONISTS =DEFEROXAMINE MESYLATE;
62. 4-Amino-7.beta.-D-ribofuranosyl-7H-pyrrolo(2, 3-d)pyrimidine
[antibiotic purine ribonucleoside that readily substitutes for adenosine in the biological system, but its incorporation into DNA and RNA has an inhibitory effect on the metabolism of these nucleic acids; an antineoplastic antimetabolite. ( CSP )] (UMLS (NCI) C0041286) =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance ;
=antifungal antibiotic;
antineoplastic antibiotics;
antitubercular agent;
ribonucleoside;
nucleoside analog;
13. 1-Aminocyclopentane
[A synthetic amino acid derivative of cyclopentanecarboxylic acid, Cycloleucine displays immunosuppressive, antineoplastic, and cytostatic properties. Believed to act in vivo as a valine antagonist and an NMDA receptor antagonist acting at the glycine site, Cycloleucine is a competitive inhibitor of many enzymes, such as methionine adenosyltransferase (S-adenosylmethionine biosynthesis). Toxicity is correlated with a block of nucleic acid methylation; cell cycle progression; and DNA, RNA and protein biosynthesis. (NCI04) ( NCI )] (UMLS (NCI) C0010575) =Amino Acid, Peptide, or Protein; Pharmacologic Substance
63. 4-Amino-N-(3,4-dimethyl-5-isoxazolyl)benzenesulfonamide
[A broad-spectrum, short-acting sulfanilamide and a synthetic analog of para-aminobenzoic acid (PABA) with antibacterial property. Sulfisoxazole competes with PABA for the bacterial enzyme dihydropteroate synthase, thereby preventing the incorporation of PABA into dihydrofolic acid, the immediate precursor of folic acid. This leads to an inhibition of bacterial folic acid synthesis and de novo synthesis of purines and pyrimidines, ultimately resulting in cell growth arrest and cell death. ( NCI )] (UMLS (NCI) C0038745) =Organic Chemical; Pharmacologic Substance ;
=Sulfanilamides;
[AM650] SULFONAMIDE/RELATED ANTIMICROBIALS =SULFISOXAZOLE DIOLAMINE;
Acetamide, N-((4-aminophenyl)sulfonyl)-N-(3,4-dimethyl-5-isoxazolyl)-;
SULFISOXAZOLE DIOLAMINE;
Acetamide, N-((4-aminophenyl)sulfonyl)-N-(3,4-dimethyl-5-isoxazolyl)-;
SULFISOXAZOLE 500 MG;
SULFISOXAZOLE 600 MG;
SULFISOXAZOLE 10 %;
SULFISOXAZOLE 15 %
14. 16-(3-Amino-3,6-didesoxy-beta-D-mannopyranosyloxy)-5,6-epoxy-8,12,14-trihydroxy-26-methyl-2,10-dioxo-1-oxacyclohexacosa-3,17,19,21,23-pentaen-13-carbonsaeure
[A polyene amphoteric macrolide antibiotic with antifungal properties. Natamycin exerts its antifungal effects by binding to sterols in the fungal cell membrane thereby increasing membrane permeability. This leads to a leakage and loss of essential cellular constituents. Following ocular application, natamycin is retained in the conjunctival fornices and attains effective concentrations within the corneal stroma where it exerts its effect. ( NCI )] (UMLS (NCI) C0027444) =Organic Chemical; Antibiotic =macrolide antibiotic;
[OP202] ANTIFUNGALS, TOPICAL OPHTHALMIC =NATAMYCIN 5 %WV;
64. 4-Aminobenzenesulfonamide
[potent antibacterial agent, the first of the sulfonamides discovered. ( CSP )] (UMLS (NCI) C0038702) =Organic Chemical; Antibiotic =Sulfanilamides;
benzenesulfonamide;
antibacterial agent;
[GU300] ANTI-INFECTIVES, VAGINAL =Benzenesulfonamide, 4-amino-N-(5-methyl-3-isoxazolyl)-;
SULFANILAMIDE 1.05 GM;
SULFANILAMIDE 15 %;
15. 17am
[Mandibular left third molar abutment mesial hemisection ( HL7V3.0 )] (UMLS (HL7) C1553650) =Medical Device =Artificial dentition;
65. 4-Aminofolic acid
[folic acid derivative used as a rodenticide that has been shown to be teratogenic. ( CSP )] (UMLS (NCI) C0002583) =Organic Chemical; Hazardous or Poisonous Substance
16. 18am
[Mandibular left second molar abutment mesial hemisection ( HL7V3.0 )] (UMLS (HL7) C1553653) =Medical Device =Artificial dentition;
66. 5 aminolevulinate synthase
[An enzyme of the transferase class that catalyzes condensation of the succinyl group from succinyl coenzyme A with glycine to form delta-aminolevulinate. It is a pyridoxyal phosphate protein and the reaction occurs in mitochondria as the first step of the heme biosynthetic pathway. The enzyme is a key regulatory enzyme in heme biosynthesis. In liver feedback is inhibited by heme. EC 2.3.1.37. ( MSH )] (UMLS (CSP) C0002565) =Amino Acid, Peptide, or Protein; Enzyme ;
17. 19am
[Mandibular left first molar abutment mesial hemisection ( HL7V3.0 )] (UMLS (HL7) C1553656) =Medical Device =Artificial dentition;
67. 5'-[(3-Amino-3-carboxypropyl)methylsulfonio]-5'-deoxyadenosine Hydroxide, Inner Salt
[physiologic methyl radical donor involved in enzymatic transmethylation reactions and present in all living organisms; possesses anti-inflammatory activity and has been used in treatment of chronic liver disease. ( CSP )] (UMLS (NCI) C0036002) =Amino Acid, Peptide, or Protein; Pharmacologic Substance; Biologically Active Substance =adenosine;
L-Methionine;
high energy compound;
18. 2 amino 4 phosphonobutyrate
[ ] (UMLS (CSP) C0206979) =Organic Chemical; Pharmacologic Substance ;
68. 5-Amino-2-hydroxybenzoic Acid
[An agent derived from sulfasalazine, an antiinflammatory agent. Mesalamine may reduce inflammation through inhibition of cyclooxygenase and prostaglandin production. Following rectal or oral administration, only a small amount of mesalamine is absorbed; the remainder, acting topically, reduces bowel inflammation, diarrhea, rectal bleeding and stomach pain. (NCI04) ( NCI )] (UMLS (NCI) C0127615) =Amino Acid, Peptide, or Protein; Pharmacologic Substance ;
=Aminosalicylic Acids;
[GA900] GASTRIC MEDICATIONS, OTHER;
[RS100] ANTI-INFLAMMATORIES, RECTAL;
=MESALAMINE 250 MG;
MESALAMINE 500 MG;
MESALAMINE 400 MG;
MESALAMINE 4 GM/60ML
19. 2-((Aminocarbonyl)oxy)-N,N,N-trimethylethanaminium Chloride
[slowly hydrolyzed cholinergic agonist that acts at both muscarinic and nicotinic receptors. ( CSP )] (UMLS (NCI) C0006945) =Organic Chemical; Pharmacologic Substance =choline;
cholinergic agent;
[OP102] MIOTICS, TOPICAL OPHTHALMIC;
[OP109] ANTIGLAUCOMA, OTHER =CARBACHOL 0.75 %WV;
CARBACHOL 1.5 %;
CARBACHOL 2.25 %;
CARBACHOL 3 %;
CARBACHOL 0.01 %
69. 5-Amino-6-(70-amino-5,8-dihydro-6-methoxy-5,8-dioxo-2-quinolyl)-4-(2-hydroxy-3,4-dimethoxyphenyl)-3-methylpicolinic Acid
[An aminoquinone antineoplastic antibiotic isolated from the bacterium Streptomyces flocculus. Streptonigrin complexes with DNA and topoisomerase II, resulting in DNA cleavage and inhibition of DNA replication and RNA synthesis. This agent also acts as a reverse transcriptase inhibitor and causes free radical-mediated cellular damage. (NCI04) ( NCI )] (UMLS (NCI) C0038427) =Organic Chemical; Antibiotic ;
20. 2-(1-(Ammoniocarbonyl)-3-(diisopropylammonio)-1-phenylpropyl)pyridinium Phosphate
[A class Ia antiarrhythmic agent with cardiac depressant properties. Disopyramide phosphate exerts its actions by blocking both sodium and potassium channels in cardiac membrane during phase 0 of the action potential. This slows the impulse conduction through the AV node and prolongs the duration of the action potential of normal cardiac cells in atrial and ventricular tissues. Disopyramide prolongs the QT interval and causes a widening of the QRS complex. It also posesses some anticholinergic and local anaesthetic properties. Disopyramide phosphate is used in the treatment of supraventricular tachycardia. ( NCI )] (UMLS (NCI) C0700534) =Organic Chemical; Pharmacologic Substance =disopyramide;
=DISOPYRAMIDE PHOSPHATE 100 MG;
DISOPYRAMIDE PHOSPHATE 150 MG;
70. 6 aminonicotinamide
[A synthetic analogue and nicotinamide antagonist with cytotoxic properties, 6-Aminonicotinamide forms an abnormal NAD (ubiquitous metabolic pathway coenzyme) analog that inhibits NAD-dependent enzyme activity associated with ATP production. 6-Aminonicotinamide impairs cartilage formation, may have teratogenic effects, and enhances the effect of radiation and cisplatin treatment (formation of platinum-DNA complexes). (NCI04) ( NCI )] (UMLS (CSP) C0000610) =Organic Chemical; Pharmacologic Substance; Vitamin; Hazardous or Poisonous Substance
21. 2-(2-Amino-3-methoxyphenyl)-4H-1-benzopyran-4-one
(UMLS (NCI) C0380453) =Organic Chemical; Pharmacologic Substance ;
71. 6-Aminocaproic Acid
[A synthetic lysine derivative with antifibrinolytic activity. Aminocaproic acid competitively inhibits activation of plasminogen, thereby reducing conversion of plasminogen to plasmin (fibrinolysin), an enzyme that degrades fibrin clots as well as fibrinogen and other plasma proteins including the procoagulant factors V and VIII. Aminocaproic acid competitively reduces the conversion of plasminogen to plasmin by plasminogen activators. It directly inhibits proteolytic activity of plasmin, but higher doses are required than are needed to reduce plasmin formation. Aminocaproic acid is used in the treatment of hemorrhage and prophylactically against hemorrhage, including hyperfibrinolysis-induced hemorrhage and postsurgical hemorrhage. ( NCI )] (UMLS (NCI) C0000608) =Amino Acid, Peptide, or Protein; Pharmacologic Substance
22. 2-Amino 6MP
[thioguanine is USP. ( CSP )] (UMLS (NCI) C0039902) =Organic Chemical; Pharmacologic Substance ;
=1,7-Dihydro-6H-purine-6-thione;
[AN300] ANTINEOPLASTICS, ANTIMETABOLITES;
[AN000] ANTINEOPLASTICS;
purine;
guanine analog;
=THIOGUANINE 40 MG
72. 8-Aminoisoindolo(1,2-b)quinazolin-12(10H)-one
[A water insoluble heterocyclic amide with potential antineoplastic activity. Batracylin appears to intercalate into DNA and interferes with topoisomerase II activity, thereby inhibiting DNA replication and repair, and RNA and protein synthesis. The acetylated form of batracylin is highly toxic and capable of inducing unscheduled DNA synthesis. This agent should, therefore, only be administered in patients with a slow acetylator NAT-2 genotype. ( NCI )] (UMLS (NCI) C0053006) =Organic Chemical; Pharmacologic Substance
23. 2-Amino, 6-Methoxypurine Arabinoside
[An arabinonucleoside antimetabolite with antineoplastic activity. Nelarabine is demethoxylated by adenosine deaminase to become biologically active 9-beta-D-arabinosylguanine (ara-G); ara-G incorporates into DNA, thereby inhibiting DNA synthesis and inducing an S phase-dependent apoptosis of tumor cells. (NCI04) ( NCI )] (UMLS (NCI) C0907349) 2-Amino-6-methoxypurine arabinoside;
2-Amino-9-beta-D-arabinofuranosyl-6-methoxy-9H-purine;
NELARABINE;
Nelarabine Intravenous Injection =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance ;
73. 9-amino-20(S)-camptothecin
(UMLS (NCI) C0950849) 9-Amino-20-(S)-camptothecin =Organic Chemical; Pharmacologic Substance
24. 2-Amino-1,3-Dihydroxyoctadecane
[A saturated derivative of sphingosine. As an inhibitor of protein kinase C (PKC), L-threo-dihydrosphingosine competitively binds to the regulatory phorbol-binding domain of PKC, a kinase involved in tumorigenesis. This agent has been shown to act synergistically with other chemotherapeutic agents and may potentiate chemotherapy drug-induced apoptosis in vitro and in vivo. Check for "http://www.cancer.gov/Search/ClinicalTrialsLink.aspx?id=41910&idtype=1" active clinical trials or "http://www.cancer.gov/Search/ClinicalTrialsLink.aspx?id=41910&idtype=1&closed=1" closed clinical trials using this agent. ("http://nciterms.nci.nih.gov:80/NCIBrowser/ConceptReport.jsp?dictionary=NCI_Thesaurus&code=C1568" NCI Thesaurus) ( PDQ )] (UMLS (NCI) C0074987) =Lipid; Pharmacologic Substance ;
74. A-MethaPred
(UMLS (NCI) C0701467) =Steroid; Pharmacologic Substance; Hormone
25. 2-Amino-1,7-dihydro-6H-purin-6-one
[2-amino-6-hydroxypurine; one of the 5 major bases (with adenine, thymine, cytosine, and uracil) found in nucleic acids. ( CSP )] (UMLS (NCI) C0018321) =Nucleic Acid, Nucleoside, or Nucleotide; Biologically Active Substance =2-Aminopurine;
Hypoxanthines;
nucleobase;
=2-Amino-1,9-dihydro-9-[(2-hydroxyethoxy)methyl]-6H-purin-6-one
75. A-Microtubule
(UMLS (NCI) C1510674) =Cell Component ;
26. 2-Amino-1,9-dihydro-9-[(2-hydroxyethoxy)methyl]-6H-purin-6-one
[9-(2-hydroxyethoxymethyl) guanine; acts against herpesviruses by inhibiting the viral DNA polymerase. ( CSP )] (UMLS (NCI) C0001367) =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance ;
76. A-myb Messenger RNA Overexpression
(UMLS (NCI) C1510675) A-myb mRNA Overexpression;
=Cell or Molecular Dysfunction ;
27. 2-Amino-1,9-[[2-hydroxy-1-(hydroxymethyl)ethoxy]methyl]-6H-purin-6-one
[9-(1,3-dihydroxy-2-propoxy)methylguanine; acyclovir analog which inhibits DNA replication of CMV and therefore has efficacy against AIDS-related oculopathy. ( CSP )] (UMLS (NCI) C0017066) =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance =2-Amino-1,9-dihydro-9-[(2-hydroxyethoxy)methyl]-6H-purin-6-one;
[AM800] ANTIVIRALS;
2-Amino-1,9-[[2-hydroxy-1-(hydroxymethyl)ethoxy]methyl]-6H-purin-6-one;
[OP203] ANTIVIRALS, TOPICAL OPHTHALMIC;
nucleoside analog;
=2-Amino-1,9-[[2-hydroxy-1-(hydroxymethyl)ethoxy]methyl]-6H-purin-6-one;
DHPG sodium;
GANCICLOVIR 500 MG;
GANCICLOVIR 4.5 MG;
77. A10/MTX
(UMLS (NCI) C0796429) Antineoplaston A10/Methotrexate =Therapeutic or Preventive Procedure
28. 2-Amino-1-Methyl-6-Phenylimidazo[4,5-b]Pyridine
[A synthetic, gray-white crystalline solid that is soluble in dimethylsulfoxide and methanol. It is produced in small quantities for research purposes. 2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine is formed naturally during the cooking of muscle-derived foods (meat and fish). Levels of this chemical produced in this manner are dependent on cooking temperature, cooking time and method of cooking (direct or indirect). It is one of the most abundant heterocyclic amines in a typical Western diet. 2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine has also been detected in processed food flavorings, beer, wine, and cigarette smoke. It is reasonably anticipated to be a human carcinogen. (NCI05) ( NCI )] (UMLS (NCI) C0045811) =Organic Chemical; Hazardous or Poisonous Substance ;
78. AM
[Every morning at institution specified times. ( HL7V3.0 )] (UMLS (HL7) C0332170) =Temporal Concept =GTSAbbreviation;
29. 2-Amino-3,4-Dimethylimidazole[4,5-f]quinoline
[A synthetic, yellow-green crystalline solid that is soluble in dimethylsulfoxide and methanol. It is produced in small quantities for research purposes. 2-Amino-3,4-dimethylimidazo[4,5-f]quinoline is formed naturally during the cooking of muscle-derived foods (meat and fish). Levels of this chemical produced in this manner are dependent on cooking temperature, cooking time and method of cooking (direct or indirect). 2-Amino-3-methylimidazo[4,5-f]quinoline has also been detected in processed food flavorings, beer, wine, and cigarette smoke. It is reasonably anticipated to be a human carcinogen. (NCI05) ( NCI )] (UMLS (NCI) C0045819) =Organic Chemical; Hazardous or Poisonous Substance ;
79. Am
[completely man-made radioactive actinide with atomic symbol Am; because of its nonmagnetic ground state, it is an excellent superconductor; it is also used in bone mineral analysis and as a radiation source for radiotherapy. ( CSP )] (UMLS (NCI) C0002467) =Pharmacologic Substance; Element, Ion, or Isotope
30. 2-Amino-3,8-dimethylimidazo[4,5-f]quinoxaline
[A synthetic, pale orange to brown crystalline solid that is soluble in dimethylsulfoxide and methanol. It is produced in small quantities for research purposes. 2-Amino-3,8-dimethylimidazo[4,5-f]quinoxaline is formed naturally during the cooking of muscle-derived foods (meat and fish). Levels of this chemical produced in this manner are dependent on cooking temperature, cooking time and method of cooking (direct or indirect). It is one of the most abundant heterocyclic amines in a typical Western diet. 2-Amino-3,8-dimethylimidazo[4,5-f]quinoxaline has also been detected in processed food flavorings, beer, wine, and cigarette smoke. It is reasonably anticipated to be a human carcinogen. (NCI05) ( NCI )] (UMLS (NCI) C0045822) =Organic Chemical; Pharmacologic Substance; Hazardous or Poisonous Substance
80. AM
[A country in Southwestern Asia, east of Turkey. (NCI) ( NCI )] (UMLS (NCI) C0003798) =Geographic Area ;
31. 2-Amino-3-(5-hydroxy-1-H-indol-3-yl)propionic Acid
[precursor of serotonin used as antiepileptic and antidepressant. ( CSP )] (UMLS (NCI) C0000578) =Amino Acid, Peptide, or Protein; Pharmacologic Substance; Biologically Active Substance
81. AMA
[A voluntary membership organization of physicians that sets standards for the profession of medicine, and is highly focused on medical education. Publishes JAMA, the Journal of the American Medical Association. ( NCI )] (UMLS (NCI) C0002461) =Professional Society ;
32. 2-Amino-3-hydroxypropionic Acid
[naturally occurring nonessential aminoacid, chemical name 2-amino-3-hydroxypropionic acid; it may be synthesized from glycine or threonine and is involved in the biosynthesis of purines, pyrimidines, and other amino acids. ( CSP )] (UMLS (NCI) C0036720) =Amino Acid, Peptide, or Protein; Pharmacologic Substance; Biologically Active Substance =Amino Acids, Neutral;
hydroxyaminoacid;
primary aminoacid;
Inactive Ingredient Preparations;
Unclassified Ingredient Preparations;
=(+)-4-Amino-3-isoxazolidinone;
SERINE 0.33 GM;
SERINE 0.5 GM;
SERINE 1.86 MG/ML;
SERINE 147 MG/100ML;
SERINE 150 MG/100ML;
SERINE 180 MG;
SERINE 2.21 MG/ML;
SERINE 2.25 MG/ML;
SERINE 2.65 MG/ML;
SERINE 20 MG;
SERINE 210 MG/100ML;
SERINE 230 MG/100ML;
SERINE 3 MG/ML;
SERINE 3.7 MG/ML;
SERINE 3.71 MG/ML;
SERINE 300 MG;
SERINE 347 MG/100ML;
SERINE 370 MG;
SERINE 4.5 MG/ML;
SERINE 4.95 MG/ML;
SERINE 420 MG/100ML;
SERINE 5 MG;
SERINE 5.3 MG/ML;
SERINE 5.92 MG/ML;
SERINE 500 MG;
SERINE 500 MG/100ML;
SERINE 56 MG/GM;
SERINE 590 MG/100ML;
SERINE 795 MG/100ML
82. AMA
(UMLS (NCI) C0279755) =Therapeutic or Preventive Procedure
33. 2-Amino-3-methylimidazo[4,5-f]quinoline
[A synthetic, light tan crystalline solid that is soluble in dimethylsulfoxide and methanol. It is produced in small quantities for research purposes. 2-Amino-3-methylimidazo[4,5-f]quinoline is formed naturally during the cooking of muscle-derived foods (meat and fish). Levels of this chemical produced in this manner are dependent on cooking temperature, cooking time and method of cooking (direct or indirect). 2-Amino-3-methylimidazo[4,5-f]quinoline has also been detected in processed food flavorings, beer, wine, and cigarette smoke. It is reasonably anticipated to be a human carcinogen. (NCI05) ( NCI )] (UMLS (NCI) C1312059) 3-Methyl-3H-imidazo[4,5-f]quinolin-2-amine;
IQ =Organic Chemical; Pharmacologic Substance; Hazardous or Poisonous Substance
83. Amacrine Cell
[interneurons of the vertebrate retina which integrate, modulate, and interpose a temporal domain in the visual message presented to the retinal ganglion cells, with which they synapse in the inner plexiform layer. ( CSP )] (UMLS (NCI) C0229216) =Cell =nerve cell;
Eye - Retina (MMHCC)
34. 2-Amino-4-(S-butylsulfonimidoyl) Butanoic Acid
[used as a thiol depleter and inhibitor of the enzyme gamma glutamylcysteine synthase. ( CSP )] (UMLS (NCI) C0054252) =Amino Acid, Peptide, or Protein; Pharmacologic Substance; Hazardous or Poisonous Substance =Amino Acids, Sulfur;
sulfhydryl reagent
84. Amalgam
[An alloy, typically a mix of silver, tin, and mercury, used in direct dental restorations. ( NCI )] (UMLS (NCI) C0440138) =Biomedical or Dental Material; Inorganic Chemical
35. 2-Amino-5-(carbamoylamino)pentanoic Acid
[amino acid, C6H13N3O3, originally isolated from watermelon, that is produced as an intermediate in the conversion of ornithine to arginine during urea formation in the liver; chemical name L-ornithine, N5-(aminocarbonyl). ( CSP )] (UMLS (NCI) C0008864) =Amino Acid, Peptide, or Protein; Biologically Active Substance =aa;
85. amanita toxin
[ ] (UMLS (CSP) C1113659) =Organic Chemical; Biologically Active Substance; Hazardous or Poisonous Substance
36. 2-amino-5-bromo-6-phenyl-4-(3H)-pyrimidinone
[An oral immunostimulant that causes the body to produce interferon and other substances. ( NCI )] (UMLS (NCI) C0054150) =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance
86. amanitine
[Cyclic peptides extracted from carpophores of various mushroom species. They are potent inhibitors of RNA polymerases in most eukaryotic species, blocking the production of mRNA and protein synthesis. These peptides are important in the study of transcription. Alpha-amanitin is the main toxin from the species Amanitia phalloides, poisonous if ingested by humans or animals. ( MSH )] (UMLS (CSP) C0002402) =Amino Acid, Peptide, or Protein; Hazardous or Poisonous Substance ;
37. 2-Amino-5-chlorotoluene
[A yellowish to pinkish colored, synthetic leaflet material. p-Chloro-o-toluidine is used in industry in the manufacture of azo dyes and is used in the production of the pesticide chlordimeform. This substance is a possible mutagen and is reasonably anticipated to be a human carcinogen that may be associated with an increased risk of bladder cancer. (NCI05) ( NCI )] (UMLS (NCI) C0048164) =Organic Chemical; Pharmacologic Substance
87. amantadine
[antiviral that is used in the prophylactic or symptomatic treatment of influenza A; it is also used as an antiparkinsonian agent, to treat extrapyramidal reactions, and for postherpetic neuralgia. ( CSP )] (UMLS (CSP) C0002403) =Organic Chemical; Pharmacologic Substance
38. 2-Amino-6-(trifluoromethoxy)benzothiazole
[A benzathiozole derivative with neuroprotective property. Although the mechanism of action has not been fully elucidated, riluzole may protect neural tissue by inhibiting glutamate release from presynaptic endings in the central nervous system. The agent also blocks postsynaptic NMDA-kainate-type glutamate receptors and inhibits voltage-dependent sodium channels. The inhibition of glutamatergic neurotransmission results in muscle relaxation and sedative effects. ( NCI )] (UMLS (NCI) C0073379) =Organic Chemical; Pharmacologic Substance ;
=thiazole;
[CN900] CNS MEDICATIONS, OTHER =RILUZOLE 50 MG
88. Amantadine HCl
[The hydrochloride salt form of amantadine, a synthetic tricyclic amine with antiviral, antiparkinsonian, and antihyperalgesic activities. Amantadine appears to exert its antiviral effect against the influenza A virus by interfering with the function of the transmembrane domain of the viral M2 protein, thereby preventing the release of infectious viral nucleic acids into host cells. Furthermore, this agent prevents virus assembly during virus replication. Amantadine exerts its antiparkinsonian effects by stimulating the release of dopamine from striatal dopaminergic nerve terminals and inhibiting its pre-synaptic reuptake. This agent may also exert some anticholinergic effect through inhibition of N-methyl-D-aspartic acid (NMDA) receptor-mediated stimulation of acetylcholine, resulting in antihyperalgesia. ( NCI )] (UMLS (NCI) C0936072) AMANTADINE HYDROCHLORIDE;
AMANTADINE HYDROCHLORIDE PREPARATION =Organic Chemical; Pharmacologic Substance ;
=amantadine;
=AMANTADINE HYDROCHLORIDE 50 MG/5ML;
AMANTADINE HYDROCHLORIDE 100 MG
39. 2-Amino-9,10-anthracenedione
[A synthetic, red or orange-brown needle-shaped solid that is insoluble in water and soluble in alcohol, acetone, benzene and chloroform. It is used as intermediate for the synthesis of both anthraquinone dyes and pharmaceutical products. When 2-aminoanthraquinone is heated to decomposition, it emits toxic fumes of nitrogen oxides. The primary route of potential human exposure to this chemical is dermal contact. Acute exposure of humans to 2-aminoanthraquinone can cause irritation of the eyes and skin. It is reasonably anticipated to be a human carcinogen. (NCI05) ( NCI )] (UMLS (NCI) C0045870) =Organic Chemical; Hazardous or Poisonous Substance ;
89. Amapari virus
[ ] (UMLS (CSP) C0002405) =Virus ;
40. 2-Aminonaphthalene
[A synthetic, air-sensitive, colorless crystalline solid that is soluble in hot water, alcohol, ether and many organic solvents. Currently, it is only used in laboratory research. Because the commercial production and use of 2-naphthylamine are banned, the potential for human exposure is low. The general population may be exposed to this chemical through inhalation of emissions from sources where nitrogen-containing organic matter is burned, such as coal furnaces and cigarettes. At greatest risk of occupational exposure to 2-naphthylamine are laboratory technicians and scientists who use it in research. Acute inhalation exposure to high levels of 2-naphthylamine can result in methemoglobinemia, dyspnea, ataxia, hematuria, dysuria and hemorrhagic cystitis. It is known to be a human carcinogen. (NCI05) ( NCI )] (UMLS (NCI) C0000300) =Organic Chemical; Hazardous or Poisonous Substance ;
90. amaurosis
[ ] (UMLS (CSP) C0376288) =Disease or Syndrome
41. 2-Aminotoluene
[A synthetic, light sensitive, light yellow liquid that is slightly soluble in water and miscible with carbon tetrachloride, diethyl ether and ethanol. The hydrochloride is a synthetic, light sensitive, white crystalline powder that is soluble in dimethylsulfoxide and ethanol. o-Toluidine and o-toluidine hydrochloride are used primarily as intermediates in the manufacture of dyes and pigments. When heated to decomposition, o-toluidine emits toxic fumes of nitrogen oxides while the hydrochloride also produces hydrochloric acid. Four studies of workers exposed to o-toluidine reported an excess of bladder cancers. o-Toluidine and o-toluidine hydrochloride are reasonably anticipated to be human carcinogens. (NCI05) ( NCI )] (UMLS (NCI) C0046584) =Organic Chemical; Indicator, Reagent, or Diagnostic Aid
91. amaurotic familial idiocy
[An outdated term for Tay-Sachs disease. ( MSH )] (UMLS (CSP) C0282220) =Disease or Syndrome ;
42. 2-[(Aminocarbonyl)oxy]-N,N,N-trimethyl-1-propanaminium Chloride
[A synthetic quaternary ammonium base derivative, parasympathomimetic Bethanechol is a slowly hydrolyzed muscarinic agonist with no nicotinic effects. Generally used to increase smooth muscle tone, Bethanechol is used to treat reflux esophagitis and to initiate urination after surgery, in urinary infections, or for enlarged prostate. It may cause hypotension, cardiac rate changes, and bronchial spasms. (NCI04) ( NCI )] (UMLS (NCI) C0106169) =Organic Chemical; Pharmacologic Substance =bethanechol;
=BETHANECHOL CHLORIDE 25 MG;
BETHANECHOL CHLORIDE 10 MG;
BETHANECHOL CHLORIDE 50 MG;
BETHANECHOL CHLORIDE 5 MG;
92. AmB
[macrolide antifungal antibiotic produced by Streptomyces nodosus obtained from soil of the Orinoco river region of Venezuela. ( CSP )] (UMLS (NCI) C0002679) =Organic Chemical; Antibiotic ;
43. 3-((4-Amino-2-methyl-5-pyrimidinyl)methyl)-5-(2-hydroxyethyl)-4-m-ethylthiazolium Chloride, Monohydrochloride
[The hydrochloride salt form of thiamine, a vitamin essential for aerobic metabolism, cell growth, transmission of nerve impulses and acetylcholine synthesis. Upon hydrolysis, thiamine hydrochloride is phosphorylated by thiamine diphosphokinase to form active thiamine pyrophosphate (TPP), also known as cocarboxylase. TPP is an coenzyme for many enzymatic activities involving fatty acid, amino acid and carbohydrate metabolism. ( NCI )] (UMLS (NCI) C0770309) THIAMINE HYDROCHLORIDE;
THIAMINE HYDROCHLORIDE PREPARATION;
Vitamin B1 Hydrochloride =Organic Chemical; Pharmacologic Substance; Vitamin =[VT105] THIAMINE;
=CRITICARE HN LIQUID;
LONALAC POWDER,ORAL;
MERITENE More…
93. Ambene
(UMLS (NCI) C0051545) =Organic Chemical; Pharmacologic Substance
44. 3-(Aminocarbonyl)-O4-deacetyl-3-de-(methoxycarbonyl)vincaleukoblastine
[An anticancer drug that belongs to the family of plant drugs called vinca alkaloids. ( NCI )] (UMLS (NCI) C0042682) =Organic Chemical; Pharmacologic Substance ;
94. AMBENONIUM CHLORIDE
[The chloride salt form of ambenonium, a quaternary ammonium compound with parasympathomimetic activity. Ambenonium chloride is a rapid indirect-acting cholinergic agonist that reversibly blocks the activity of acetylcholinesterase, thereby prevents acetylcholine hydrolysis and prolonging its activity on nicotinic receptors at the neuromuscular junction. ( NCI )] (UMLS (NCI) C0002413) =Organic Chemical; Pharmacologic Substance
45. 3-(Aminomethyl)-5-methyl-hexanoic Acid
[A 3-isobutyl derivative of gamma-amino butyric acid (GABA) with anti-convulsant, anti-epileptic, anxiolytic and analgesic activities. Pregabalin selectively binds to alpha2delta (A2D) subunit of the presynaptic voltage-gated calcium channels located in the central nervous system (CNS). Binding of A2D subunits prevent calcium influxes and the subsequent calcium-dependent releases of various neurotransmitters from presynaptic nerve terminals in hyperexcited neurons, including glutamate, norepinephrine, serotonin, dopamine, and substance P. This leads to an inhibition of synaptic transmission and reduces neuronal excitability. Pregabalin does not bind directly to GABA-A, GABA-B receptors and does not alter GABA uptake or degradation. ( NCI )] (UMLS (NCI) C0657912) =Amino Acid, Peptide, or Protein; Pharmacologic Substance ;
95. Amber Acid
[A water-soluble, colorless crystal with an acid taste that is used as a chemical intermediate, in medicine, the manufacture of lacquers, and to make perfume esters. It is also used in foods as a sequestrant, buffer, and a neutralizing agent. (Hawley's Condensed Chemical Dictionary, 12th ed, p1099; McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed, p1851) ( MSH )] (UMLS (NCI) C0075429) =Organic Chemical; Pharmacologic Substance ;
=Succinic Acids;
=succinate;
46. 3-Amino-1,2,4-benzotriazine-1,4-dioxide
[antineoplastic, radiation sensitizing agent; 3-amino1,2,4-benzotriazine 1,4-dioxide. ( CSP )] (UMLS (NCI) C0208407) =Organic Chemical; Pharmacologic Substance ;
=[AN000] ANTINEOPLASTICS;
Radiation Sensitizers;
triazine;
96. Amber Bottle
[A bottle of yellow to brown color. Used to store light-sensitive materials ( HL7V3.0 )] (UMLS (HL7) C1553455) =Intellectual Product =Bottle;
47. 3-Amino-1-[4-(2 amino-1H-imidazolyl]-propanol, 2HCl
[A compound isolated from the marine sponge Pseudaxinyssa cantharella exhibiting anti-tumor activity. Studies indicate girodazole acts during the elongation/termination steps of protein synthesis, resulting in protein synthesis inhibition. (NCI) ( NCI )] (UMLS (NCI) C0119196) =Organic Chemical; Pharmacologic Substance
97. Ambient temperature
(UMLS (HL7) C1550111) =Intellectual Product =Special Handling Code;
48. 3-Aminopyridine-2-carboxaldehyde Thiosemicarbazone
[3-aminopyridine-2-carboxaldehyde thiosemicarbazone. A substance that is being studied as an anticancer drug. It belongs to the family of drugs called ribonucleotide reductase inhibitors. ( NCI )] (UMLS (NCI) C0210403) =Organic Chemical; Pharmacologic Substance ;
98. Ambient Temperature
[Keep at ambient temperature, 22 +/- 2C ( HL7V3.0 )] (UMLS (HL7) C1550576) =Human-caused Phenomenon or Process =EntityHandling;
49. 30am
[Mandibular right first molar abutment mesial hemisection ( HL7V3.0 )] (UMLS (HL7) C1553669) =Medical Device =Artificial dentition;
99. Ambiguous
(UMLS (HL7) C1549102) =Organism Attribute =Administrative Sex;
50. 31am
[Mandibular right second molar abutment mesial hemisection ( HL7V3.0 )] (UMLS (HL7) C1553672) =Medical Device =Artificial dentition;
100. AmBisome
(UMLS (NCI) C0591076) =Organic Chemical; Antibiotic

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